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Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)Phase 3NCT02027701

Extension Study of Maintenance Treatment With Subcutaneous Immunoglobulin (IgPro20) for Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

A Phase 3 study testing IgPro20 in people with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) and Polyradiculoneuropathy, Chronic Inflammatory Demyelinating, run by CSL Behring at 33 sites in 11 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study is an extension study to the pivotal study IgPro20_3003 (NCT01545076). The purpose of this extension study is to investigate the long-term treatment of CIDP with IgPro20, with regard to safety and efficacy. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
IgPro20
Could I receive a placebo?
No, everyone receives an active treatment
How many people
82 participants
Where
33 sitesin 11 countries
Study dates
30 Jul 2014to 10 Jul 2017
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Subjects having completed the pivotal study IgPro20_3003 (SC Week 25) or successfully rescued from a CIDP relapse during the SC Treatment Period of pivotal study IgPro20_3003 (NCT01545076).
  • Written informed consent for study participation obtained before undergoing any study-specific procedures.

Who cannot join

  • Subject is unable to directly transition from study IgPro20_3003.
  • New medical condition and/or social behavior (ie, alcohol, drug, or medication abuse) during participation in study IgPro20_3003 that in the judgment of the investigator could increase risk to the subject, interfere with the evaluation of investigational medicinal product, and/or conduct of the study.

Trial locations and contacts

33 sites in 11 countries.

33 sites in 11 countries

Germany9 sites
  • Site Reference 2760069

    Berlin, 10117

  • Site Reference 2760072

    Berlin, 12200

  • Site Reference 2760049

    Bochum, 44791

  • Site Reference 2760052

    Essen, North Rhine-Westphalia, 45117

  • Site Reference 2760094

    Essen, 45147

  • Site Reference 2760054

    Hanover, 30625

  • Site Reference 2760055

    Leipzig, DE04103

  • Site Reference 2760047

    Potsdam, 14471

  • Site Reference 2760039

    Würzburg, 97080

Other trials in Germany

Japan6 sites
  • Site Reference 3920038

    Chiba, 260-8677

  • Site Reference 3920061

    Kanagawa, 228-8555

  • Site Reference 3920040

    Nagoya, 466-8560

  • Site Reference 3920037

    Tokorozawa, Saitama, 359-8513

  • Site Reference 3920065

    Tokyo, 113-8431

  • Site Reference 3920035

    Ube, Yamaguchi, 755-8505

Other trials in Japan

United States5 sites
  • Site Reference 8400181

    Birmingham, Alabama, 35294-0017

  • Site Reference 8400182

    Charlotte, North Carolina, 28210

  • Site Reference 8400166

    Kansas City, Kansas, 66160

  • Site Reference 8400167

    Los Angeles, California, 90033

  • Site Reference 8400169

    New York, New York, 10021

Other trials in United States

Australia2 sites
  • Site Reference 0360011

    Fitzroy, Victoria, 3065

  • Site Reference 0360017

    Woolloongabba, Queensland, 4102

Other trials in Australia

Canada2 sites
  • Site Reference 1240007

    Greenfield Park, Quebec, J4V2J2

  • Site Reference 1240009

    Toronto, Ontario, M5G 2C4

Other trials in Canada

Czechia2 sites
  • Site Reference 2030009

    Hradec Králové, 50003

  • Site Reference 2030002

    Hradec Králové, 50005

Other trials in Czechia

Spain2 sites
  • Site Reference 7240011

    Barcelona, 08035

  • Site Reference 7240010

    Barcelona, 08907

Other trials in Spain

United Kingdom2 sites
  • Site Reference 8260019

    London, WC1N 3BG

  • Site Reference 8260032

    Salford, M6 8HD

Other trials in United Kingdom

France1 site
  • Site Reference 2500022

    Nice, 06002

Other trials in France

Italy1 site
  • Site Reference 3800031

    Milan, 20133

Other trials in Italy

Netherlands1 site
  • Site Reference 5280001

    Amsterdam, 1105

Other trials in Netherlands

About this study

Official title: Multicenter, Open-label Extension Study to Investigate the Long-term Safety and Efficacy of IgPro20 in Maintenance Treatment of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) in Subjects Completing Study IgPro20_3003

This study is an extension study to the pivotal study IgPro20_3003 (NCT01545076). The purpose of this extension study is to investigate the long-term treatment of CIDP with IgPro20, with regard to safety and efficacy.

Subjects who have completed subcutaneous (SC) Week 25 or were successfully rescued from a CIDP relapse during the SC Treatment Period of pivotal study IgPro20_3003 (NCT01545076) will have the option to receive open-label low-dose IgPro20 (0.2 g/kg bodyweight [bw]) weekly for up to 48 weeks. Subjects relapsing on low-dose IgPro20 will either return to high-dose IgPro20 (0.4 g/kg) immediately or be discontinued, depending on investigator's judgment. Subjects returning to high-dose IgPro20 will continue on high-dose until they have completed a total of 48 weeks of IgPro20 treatment. If subjects do not successfully recover from CIDP relapse within 4 weeks, they will be withdrawn.

The treatment duration will be up to 48 weeks, followed by a completion visit (week 49).

Being tested
IgPro20
Medical subject headings
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • IgPro20Biological

Study groups in NCT02027701
Study groupRoleWhat they receive
IgPro20Experimental20% liquid formulation (200 mg/mL) of human normal immunoglobulin for SC use administered SC weekly: 0.2 g/kg bw (low-dose IgPro20) for up to 48 weeks. Subjects who experience CIDP relapse on 0.2 g/kg IgPro20 will have an increase to 0.4 g/kg IgPro20 immediately and will continue on high-dose until they have completed a total of 48 weeks of IgPro20 treatment.
Receives: Biological: IgPro20

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Adverse Events (AEs) Per Infusion

    Measured: Up to 49 weeks

Secondary outcomes (12)
  1. Time to First CIDP Relapse

    Time to first CIDP relapse based on adjusted INCAT score, using the Kaplan-Meier estimator. Relapse is defined as an increase of at least 1 INCAT score point (except for the increase from 0 to 1 in the upper limb score only).

    Measured: Up to 49 weeks

  2. Change From Baseline in CIDP Total Adjusted Inflammatory Neuropathy Cause and Treatment (INCAT) Score

    The INCAT score is a 10-point scale that covers the functionality of legs and arms, and has been successfully used to measure treatment effects in various CIDP studies. Scores for arm disability range from 0 ("No upper limb problems") to 5 ("Inability to use either arm for any purposeful movement"), and scores for leg disability range from 0 ("Walking not affected") to 5 ("Restricted to wheelchair, unable to stand and walk a few steps with help"). The INCAT (total) score is the sum of these 2 scores and ranges from 0 to 10. For the "adjusted" INCAT score, changes in the function of the upper limbs from 0 (normal) to 1 (minor symptoms) or from 1 to 0 were not recorded as deterioration or improvement because these changes are not considered clinically significant.

    Measured: Baseline and up to 49 weeks

  3. Change From Baseline in Medical Research Council (MRC) Score

    An adapted version of the MRC sum score as published by Kleyweg and the RMC trial group was used. With the MRC sum score, the following 8 bilateral muscle pairs were assessed, and individual muscle scores as well as the sum score documented: Shoulder abduction; Elbow flexion; Wrist extension; Index finger abduction; Hip flexion; Knee extension; Foot dorsiflexion; Great toe dorsiflexion. The MRC sum score ranges from 0 (paralysis) to 80 (normal strength) points.

    Measured: Baseline and up to 49 weeks

  4. Change From Baseline in Rasch-built Overall Disability Scale (R-ODS)

    The R-ODS is a recently published outcome measure that captures activity and social participation in subjects with Guillain-Barré Syndrome, CIDP, and monoclonal gammopathy of uncertain significance. The 24-item questionnaire covers a wide range of tasks of daily life that are each to be rated as "impossible to perform", "able to perform with difficulty", or "easy to perform" (scale of 0 - 2 points respectively). Items are sorted in order of increasing difficulty to perform, based on data from subjects with peripheral neuropathies (chronic inflammatory demyelinating polyneuropathy, Guillain-Barré Syndrome, or monoclonal gammopathy of uncertain significance) and subjects recruited at the university outpatient clinics of Rotterdam and Maastricht.

    Measured: Baseline and up to 49 weeks

  5. Change From Baseline in Mean Grip Strength

    The hand-held Vigorimeter from Martin (Tuttlingen, Germany) is a device that measures the strength of small muscles in the hand, ie, grip strength. The subject squeezes a rubber bulb lying between the palm of the hand and the thumb and index fingers. The pressure is recorded via a rubber tube on a nanometer and expressed in kilopascal (kPa). At each assessment, the subject squeezes 3 times with each hand.

    Measured: Baseline and up to 49 weeks

  6. Percentage of Subjects With Adverse Events (AEs)

    Measured: Up to 49 weeks

  7. Number of AEs by Severity Per Infusion

    Measured: Up to 49 weeks

  8. Percentage of Subjects With AEs by Severity

    Measured: Up to 49 weeks

  9. Number of Causally Related AEs Per Infusion

    Measured: Up to 49 weeks

  10. Percentage of Subjects With Causally Related AEs

    Measured: Up to 49 weeks

  11. Number of Serious AEs Per Infusion

    Measured: Up to 49 weeks

  12. Percentage of Subjects With Serious AEs

    Measured: Up to 49 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Jan 2014 (estimated)
  2. Study start30 Jul 2014
  3. Primary completion10 Jul 2017
  4. Study completion10 Jul 2017

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
82 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02027701
Sponsor's protocol ID
IgPro20_3004
Other IDs
2013-004157-24
Status last verified
Sep 2018
First submitted
3 Jan 2014
Last updated
2 Oct 2018
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing IgPro20 in people with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) and Polyradiculoneuropathy, Chronic Inflammatory Demyelinating, run by CSL Behring at 33 sites in 11 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Oct 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 33 sites in Germany, Japan, United States, Australia, Canada and 6 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 2 Oct 2018). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Adverse Events (AEs) Per Infusion (time frame: Up to 49 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Oct 2018.

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